ArticleJournal of neuro-oncology2025
Vaccine-induced immunity is maintained in glioma patients relative to other solid tumours.
Article in Journal of neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Long-term cellular and humoral responses to SARS-CoV-2 vaccinations in patients with solid malignancies undergoing chemotherapy.Frontiers in immunology · 2025Article
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Authors and funding
28 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundGliomas are the most common primary brain malignancy in adults, with treatment advances limited by challenges like the blood-brain barrier, tumour heterogeneity, and an immunosuppressive microenvironment. Tumour vaccines, such as adenoviral vector and mRNA-based vaccines, may overcome these barriers, but the ability of glioma patients to mount an immune response to these therapies remains unclear. This study assesses immune responses to adenoviral DNA and mRNA-based COVID-19 vaccinations in a glioma-enriched population as a model for glioma-based vaccine therapies.
methodsCOVID-19 naïve glioma and non-glioma solid tumour patients, along with healthy volunteers, were recruited between May 2021 and December 2022. Blood samples were collected at various time points: pre-vaccination, between the first and second doses, and at 1-, 3-, and 4-6-months post 2nd vaccination, including after a third booster dose. SARS-CoV-2 specific immune responses were evaluated using ELISA and ELISPOT assays.
resultsA total of 91 participants were analysed. At 1-month post 2nd vaccination, no significant differences in seroconversion rates were observed. By 3 months, glioma and non-glioma patients had significantly lower rates compared to healthy volunteers. Memory B and T cell responses were similar between glioma patients and healthy volunteers, but non-glioma patients showed decreased responses. Vaccine efficacy was comparable across all cohorts.
conclusionThis study demonstrates that glioma patients can mount meaningful immune responses to DNA and mRNA vaccines, suggesting that glioma-based vaccine therapies are feasible and warrant further exploration.
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